FDA recall record

20-100 Delicious Seasoning Sofrito Marinating Sauce, 100% All Natural Ingredients recall — FDA F-0778-2023

Product was not stored refrigerated.

Class IIclassification
F-0778-2023official record ID
May 10, 2023report date

Recall record at a glance

Official recordF-0778-2023
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firm20-100 Delicious Seasoning LLC
Report dateMay 10, 2023
Recall initiation dateMar 9, 2023
Quantity8OZ/3 cases total 72 bottles, 16OZ/ 1 case total of 14 bottles, 32oz / 1 case total of 12 bottles
LocationMiramar, FL, United States

Official product description

Sofrito Marinating Sauce, 100% All Natural Ingredients (Caribbean Seasoning), Net Wt 16 oz. (460g), 8 oz. (230g) and 32(920g) oz. Glass Jar. Manufactured and Distributed by 20100 Seasoning LLC. Keep Refrigerated.

Why the product was recalled

Product was not stored refrigerated.

Distribution information

Domestic distribution only.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.